Evidence map›Paper›PMID 29261712›Full record

ArticlePloS one2017

Mouse decellularised liver scaffold improves human embryonic and induced pluripotent stem cells differentiation into hepatocyte-like cells.

Maëlle Lorvellec, Federico Scottoni, Claire Crowley, Rebeca Fiadeiro, Panagiotis Maghsoudlou, Alessandro Filippo Pellegata, Francesca Mazzacuva, Asllan Gjinovci, Anne-Marie Lyne, Justine Zulini and 5 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Recent Advances in Liver Engineering With Decellularized Scaffold.Frontiers in bioengineering and biotechnology · 2022
    Review
  6. Article
  7. Article
  8. Induction and Maturation of Hepatocyte-Like CellsFrontiers in cell and developmental biology · 2021
    Review
  9. AniScience · 2020
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Whole Organ Tissue Vascularization: Engineering the Tree to Develop the Fruits.Frontiers in bioengineering and biotechnology · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Maëlle LorvellecMRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.ORCID http://orcid.org/0000-0002-7566-1415
Federico ScottoniDepartment of Stem Cells and Regenerative Medicine, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Claire CrowleyDepartment of Stem Cells and Regenerative Medicine, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Rebeca FiadeiroMRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Panagiotis MaghsoudlouDepartment of Stem Cells and Regenerative Medicine, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Alessandro Filippo PellegataDepartment of Stem Cells and Regenerative Medicine, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Francesca MazzacuvaCentre for General Omics, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Asllan GjinovciDepartment of Stem Cells and Regenerative Medicine, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Anne-Marie LyneInstitut Curie, PSL Research University, Paris, France.
Justine ZuliniMRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Daniel LittleMRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Olukunbi MosakuMRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Deirdre KellyThe Liver Unit, Birmingham Children's Hospital, Birmingham, United Kingdom.
Paolo De CoppiDepartment of Stem Cells and Regenerative Medicine, Institute of Child Health and Great Ormond Street Hospital, University College London, London, United Kingdom.
Paul GissenMRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Great Ormond Street Hospital · GBMRC Laboratory for Molecular Cell Biology · GBBirmingham Children's Hospital · GBUniversité Paris Sciences et Lettres · FR

Funding

Department of Health RP_2014-04-046
6 · The paper itself

Abstract

Liver transplantation is the definitive treatment of liver failure but donor organ shortage limits its availability. Stem cells are highly expandable and have the potential to differentiate into any specialist cell. Use of patient-derived induced Pluripotent Stem Cells (hiPSCs) has the additional advantage for organ regeneration therapies by removing the need for immunosuppression. We compared hepatocyte differentiation of human embryonic stem cells (hESCs) and hiPSCs in a mouse decellularised liver scaffold (3D) with standard in vitro protocol (2D). Mouse livers were decellularised preserving micro-architecture, blood vessel network and extracellular matrix. hESCs and hiPSCs were primed towards the definitive endoderm. Cells were then seeded either in 3D or 2D cultures and the hepatocyte differentiation was continued. Both hESCs and hiPSCs differentiated more efficiently in 3D than in 2D, with higher and earlier expression of mature hepatocyte marker albumin, lipid and glycogen synthesis associated with a decrease in expression of fetal hepatocyte marker alpha-fetoprotein. Thus we conclude that stem cell hepatocyte differentiation in 3D culture promotes faster cell maturation. This finding suggests that optimised 3D protocols could allow generation of mature liver cells not achieved so far in standard 2D conditions and lead to improvement in cell models of liver disease and regenerative medicine applications.

Indexed as

Cell DifferentiationTissue ScaffoldsAnimalsEmbryonic Stem CellsExtracellular MatrixHepatocytesHumansInduced Pluripotent Stem CellsMice

Identifiers

PMID29261712
PMCPMC5738056
OpenAlexW2778870388

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.